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Difference between revisions of "User:Emil Stender"

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Emil G. P. Stender obtained his M.Sc. in biochemistry from University of Copenhagen - Denmark in 2014 and completed his PhD in 2018 at Technical University of Denmark (DTU) under supervision of [[User:Birte Svensson|Birte Svensson]] and co-supervised by Maher Abou Hachem. The project involved characterization of whey protein-alginate interactions and identification of alginate binding sites on the surface of β-lactoglobulin <cite>Stender2019 Stender2017</cite>. He has since been employed as a postdoc at DTU – Bioengineering in a project identifying and characterizing enzymes enabling human gut microbiota to utilize alginate. His main research interests are protein biophysics, [[Polysaccharide Lyases]] and alginate modifying enzymes. He published the first structure of an mannuronic acid specific alginate lyase in [[Polysaccharide Lyase Family 6]] from the human gut microbe ''Bacteroides cellulosilyticus'' <cite>Stender2019_2</cite>.   
  
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#Gilbert2008 pmid=18430603
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#Stender2019_2 pmid=31530640
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#Stender2019 Stender, E. G. P., Birch, J., Kjeldsen, C., Nielsen, L. D., Duus, J. O., Kragelund, B. B., and Svensson, B. (2019) Alginate trisaccharide binding sites on the surface of β-Lactoglobulin identified by NMR spectroscopy: implications for molecular network formation. ACS Omega. 4, 6165–6174
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#Stender2017 Stender, E. G. P., Khan, S., Ipsen, R., Madsen, F., Hägglund, P., Abou Hachem, M., Almdal, K., Westh, P., and Svensson, B. (2017) Effect of alginate size, mannuronic/guluronic acid content and pH on particle size, thermodynamics and composition of complexes with β-lactoglobulin. Food Hydrocoll. 75, 157–163
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#Stender2018 pmid=29327016
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#Stender2015 pmid=26107850
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#OShea2015 pmid=25348421
  
 
</biblio>
 
</biblio>

Latest revision as of 13:33, 18 December 2021

Emil Stender.png

Emil G. P. Stender obtained his M.Sc. in biochemistry from University of Copenhagen - Denmark in 2014 and completed his PhD in 2018 at Technical University of Denmark (DTU) under supervision of Birte Svensson and co-supervised by Maher Abou Hachem. The project involved characterization of whey protein-alginate interactions and identification of alginate binding sites on the surface of β-lactoglobulin [1, 2]. He has since been employed as a postdoc at DTU – Bioengineering in a project identifying and characterizing enzymes enabling human gut microbiota to utilize alginate. His main research interests are protein biophysics, Polysaccharide Lyases and alginate modifying enzymes. He published the first structure of an mannuronic acid specific alginate lyase in Polysaccharide Lyase Family 6 from the human gut microbe Bacteroides cellulosilyticus [3].




  1. Stender, E. G. P., Birch, J., Kjeldsen, C., Nielsen, L. D., Duus, J. O., Kragelund, B. B., and Svensson, B. (2019) Alginate trisaccharide binding sites on the surface of β-Lactoglobulin identified by NMR spectroscopy: implications for molecular network formation. ACS Omega. 4, 6165–6174

    [Stender2019]
  2. Stender, E. G. P., Khan, S., Ipsen, R., Madsen, F., Hägglund, P., Abou Hachem, M., Almdal, K., Westh, P., and Svensson, B. (2017) Effect of alginate size, mannuronic/guluronic acid content and pH on particle size, thermodynamics and composition of complexes with β-lactoglobulin. Food Hydrocoll. 75, 157–163

    [Stender2017]
  3. Stender EGP, Dybdahl Andersen C, Fredslund F, Holck J, Solberg A, Teze D, Peters GHJ, Christensen BE, Aachmann FL, Welner DH, and Svensson B. (2019). Structural and functional aspects of mannuronic acid-specific PL6 alginate lyase from the human gut microbe Bacteroides cellulosilyticus. J Biol Chem. 2019;294(47):17915-17930. DOI:10.1074/jbc.RA119.010206 | PubMed ID:31530640 [Stender2019_2]
  4. Stender EGP , Koutina G , Almdal K , Hassenkam T , Mackie A , Ipsen R , and Svensson B . (2018). Isoenergic modification of whey protein structure by denaturation and crosslinking using transglutaminase. Food Funct. 2018;9(2):797-805. DOI:10.1039/c7fo01451a | PubMed ID:29327016 [Stender2018]
  5. Stender EG, O'Shea C, and Skriver K. (2015). Subgroup-specific intrinsic disorder profiles of Arabidopsis NAC transcription factors: Identification of functional hotspots. Plant Signal Behav. 2015;10(6):e1010967. DOI:10.1080/15592324.2015.1010967 | PubMed ID:26107850 [Stender2015]
  6. O'Shea C, Kryger M, Stender EG, Kragelund BB, Willemoës M, and Skriver K. (2015). Protein intrinsic disorder in Arabidopsis NAC transcription factors: transcriptional activation by ANAC013 and ANAC046 and their interactions with RCD1. Biochem J. 2015;465(2):281-94. DOI:10.1042/BJ20141045 | PubMed ID:25348421 [OShea2015]

All Medline abstracts: PubMed